| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6933989-6934237 | Rare:69 | ||||
| chr12:7089286-7089734 | Common:3; Rare:145 | ||||
| chr12:8837317-8837526 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:8848228-8848414 | Rare:33 | ||||
| chr12:9089200-9089545 | Rare:61 | ||||
| chr12:9448208-9448303 | Common:1; Rare:44 | ||||
| chr12:12110694-12110998 | Common:2; Rare:55 | ||||
| chr12:12534739-12534896 | Rare:28 | ||||
| chr12:13202962-13203076 | Common:1; Rare:24 | ||||
| chr12:13203100-13203434 | Rare:71 | ||||
| chr12:51240770-51240972 | Rare:59 | ||||
| chr12:52032947-52033183 | Common:1; Rare:62 | ||||
| chr12:52147286-52147559 | Common:2; Rare:64 | ||||
| chr12:52280351-52280533 | Common:3; Rare:32 | ||||
| chr12:52447538-52447810 | Rare:78 |